Animal Health, AgResearch, Hopkirk Research Institute, Grasslands Research Centre, Palmerston North, New Zealand.
Food Safety & Assurance, AgResearch, Hopkirk Research Institute, Grasslands Research Centre, Palmerston North, New Zealand.
PLoS One. 2021 Feb 4;16(2):e0246573. doi: 10.1371/journal.pone.0246573. eCollection 2021.
Mycoplasma ovipneumoniae infects both sheep and goats causing pneumonia resulting in considerable economic losses worldwide. Current diagnosis methods such as bacteriological culture, serology, and PCR are time consuming and require sophisticated laboratory setups. Here we report the development of two rapid, specific and sensitive assays; an isothermal DNA amplification using recombinase polymerase amplification (RPA) and a real-time PCR for the detection of M. ovipneumoniae. The target for both assays is a specific region of gene WP_069098309.1, which encodes a hypothetical protein and is conserved in the genome sequences of ten publicly available M. ovipneumoniae strains. The RPA assay performed well at 39°C for 20 min and was combined with a lateral flow dipstick (RPA-LFD) for easy visualization of the amplicons. The detection limit of the RPA-LFD assay was nine genome copies of M. ovipneumoniae per reaction and was comparable to sensitivity of the real-time PCR assay. Both assays showed no cross-reaction with 38 other ovine and caprine pathogenic microorganisms and two parasites of ruminants, demonstrating a high degree of specificity. The assays were validated using bronchoalveolar lavage fluid and nasal swab samples collected from sheep. The positive rate of RPA-LFD (97.4%) was higher than the real-time PCR (95.8%) with DNA as a template purified from the clinical samples. The RPA assay was significantly better at detecting M. ovipneumoniae in clinical samples compared to the real-time PCR when DNA extraction was omitted (50% and 34.4% positive rate for RPA-LFD and real-time PCR respectively). The RPA-LFD developed here allows easy and rapid detection of M. ovipneumoniae infection without DNA extraction, suggesting its potential as a point-of-care test for field settings.
绵羊肺炎支原体感染绵羊和山羊,引起肺炎,在全球范围内造成了相当大的经济损失。目前的诊断方法,如细菌培养、血清学和 PCR 等,既费时又需要复杂的实验室设备。在这里,我们报告了两种快速、特异和敏感的检测方法的发展;一种是使用重组酶聚合酶扩增(RPA)的等温 DNA 扩增,另一种是用于检测绵羊肺炎支原体的实时 PCR。这两种检测方法的靶标都是基因 WP_069098309.1 的一个特定区域,该基因编码一个假定蛋白,在十个公开的绵羊肺炎支原体菌株的基因组序列中保守。RPA 检测在 39°C 下进行 20 分钟,与侧流纸条(RPA-LFD)结合,便于可视化扩增子。RPA-LFD 检测的检测限为每个反应的绵羊肺炎支原体基因组拷贝数为 9 个,与实时 PCR 检测的灵敏度相当。两种检测方法与 38 种其他绵羊和山羊致病性微生物和两种反刍动物寄生虫均无交叉反应,具有高度特异性。该检测方法使用从绵羊采集的支气管肺泡灌洗液和鼻腔拭子样本进行验证。使用从临床样本中提取的 DNA 作为模板时,RPA-LFD(97.4%)的阳性率高于实时 PCR(95.8%)。与实时 PCR 相比,当省略 DNA 提取时,RPA 检测在检测临床样本中的绵羊肺炎支原体方面明显更好(RPA-LFD 和实时 PCR 的阳性率分别为 50%和 34.4%)。这里开发的 RPA-LFD 无需 DNA 提取即可轻松快速地检测绵羊肺炎支原体感染,表明其有可能成为现场即时检测的一种方法。